MycoBiomDB – Record Details (MyCo_5567)

Biomarker Record Details

Database ID: MyCo_5567
DB IDMyCo_5567
TitleA Comprehensive in Silico Analysis of Regulatory SNPs of Human CLEC7A Gene and Its Validation as Genotypic and Phenotypic Disease Marker in Recurrent Vulvovaginal Infections
Year2018
PMID29616193
Fungal Diseases involvedVulvovaginal candidiasis
Associated Medical ConditionRecurrent Vulvovaginal infections (RVVI)
GenusNone
SpeciesNone
OrganismNone
Ethical StatementThe present study was commenced after getting approval from the Institutional Ethics Committee (Approval no. 06/HG dated 02/01/2015) of Guru Nanak Dev University, Amritsar (Punjab), India, in accordance with Indian Council of Medical Research guidelines (ICMR, 2006)modified fromWorld Medical Association (2004). Voluntary consent in written was attained from all the subjects. To ensure that subjects involved in the study had necessary information to make an informed choice the information provided to them include comprehensive depiction of the present study purpose, confirmation of secrecy of their provided information, vaginal, and blood samples collection procedures and possible risks and benefits of the study. The necessary information was recorded in a pre-designed Proforma. In addition, the bio-medical waste was segregated and managed on the basis of color coding as mentioned in Bio-Medical Waste (Management & Handling) Rules, 1998 (amended in 2000).
Site of InfectionVagina
Opportunistic invasiveNone
Sample typeBody fluid
Sample sourcePeripheral blood samples
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker NameMBL2
Biomarker Full NameMannose binding Lectin 2
Biomarker TypePredictive
BiomoleculeGene
Geographical LocationIndia
CohortThe study included 258 RVVI cases (Age, mean
Cohort No.258 Patients
Age GroupNone
P ValueNone
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismVulvovaginal infections (VVI) are the commonly reported microbiological syndrome affecting millions of women globally in all strata of society. An abnormal vaginal discharge is a key trait of VVI and its estimated prevalence in India is 30%. Bacterial Vaginosis (BV), Vulvovaginal Candidiasis (VVC), and Trichomoniasis (TV) are the three main causes of VVI. Mutual existence of these causes is termed as Mixed Infections (MI) that contribute >20% of women with VVI. Besides this, cases of recurrent VVI (RVVI) have also emerged that is commonly stated as repeated experiences of vaginal infections in a definite period, this includes recurrent VVC (RVVC) and recurrent BV (RBV). RVVC refers to ≥4 repeated episodes of VVC in 12-months while RBV refers to the repeated episodes of BV within 3 months with recurrence rates as high as 30–50%. Literature regarding RVVI pathogenesis suggests that it is caused by a fall in hydrogen peroxide producing lactobacilli and overgrowth of microbes that are either normally present in human vaginal microbiome in lower quantity or sexually transmitted. In addition, use of contraceptives, excessive antibiotics, smoking, sexual activity, immunosuppression, and black race are the other known predisposing factors that leads to RVVI. Untreated RVVI can lead to complications like infertility, pre-term birth, miscarriage, vulvovaginal inflammation, and other infectious diseases. Though diverse microbial strains have been defined in literature as a causative agent for RVVI, till date no major determinants have been recognized that could explain susceptibility to this disease condition. So, it was hypothesized that RVVI susceptibility may be determined by individual’s own genetic factors.
TechniquePCR
Analysis Methodpolymerase chain reaction-restriction fragment length polymorphism (PCR–RFLP)
ELISA kitsNone
Assay DataNone
Validation Techniques usedELISA, PCR-RFLP
Up Regulation Down RegulationDecrease
Sequence DataNone
External LinkNone